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4. Novel missense mutation found in a Japanese patient with myeloperoxidase deficiency. Ohashi YY; Kameoka Y; Persad AS; Koi F; Yamagoe S; Hashimoto K; Suzuki K Gene; 2004 Mar; 327(2):195-200. PubMed ID: 14980716 [TBL] [Abstract][Full Text] [Related]
5. Pattern of inheritance in hereditary myeloperoxidase deficiency associated with the R569W missense mutation. Nauseef WM; Cogley M; Bock S; Petrides PE J Leukoc Biol; 1998 Feb; 63(2):264-9. PubMed ID: 9468285 [TBL] [Abstract][Full Text] [Related]
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7. Insights into myeloperoxidase biosynthesis from its inherited deficiency. Nauseef WM J Mol Med (Berl); 1998 Sep; 76(10):661-8. PubMed ID: 9766843 [TBL] [Abstract][Full Text] [Related]
8. Genetic studies on myeloperoxidase deficiency in Italy. Marchetti C; Patriarca P; Solero GP; Baralle FE; Romano M Jpn J Infect Dis; 2004 Oct; 57(5):S10-2. PubMed ID: 15507752 [TBL] [Abstract][Full Text] [Related]
9. Hereditary myeloperoxidase deficiency due to a missense mutation of arginine 569 to tryptophan. Nauseef WM; Brigham S; Cogley M J Biol Chem; 1994 Jan; 269(2):1212-6. PubMed ID: 7904599 [TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the myeloperoxidase gene in a Chinese female with complete myeloperoxidase deficiency: the role of nonsense-mediated mRNA decay. Wang K; Lin B; Lin J; Lan X Gene; 2013 Feb; 515(1):205-7. PubMed ID: 23228855 [TBL] [Abstract][Full Text] [Related]
11. A novel form of hereditary myeloperoxidase deficiency linked to endoplasmic reticulum/proteasome degradation. DeLeo FR; Goedken M; McCormick SJ; Nauseef WM J Clin Invest; 1998 Jun; 101(12):2900-9. PubMed ID: 9637725 [TBL] [Abstract][Full Text] [Related]
12. [Myeloperoxidase deficiency]. Shiohara M; Komiyama A Ryoikibetsu Shokogun Shirizu; 2000; (32):183-5. PubMed ID: 11212684 [No Abstract] [Full Text] [Related]
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14. Genomic variations in myeloperoxidase gene in the Japanese population. Kameoka Y; Persad AS; Suzuki K Jpn J Infect Dis; 2004 Oct; 57(5):S12-3. PubMed ID: 15507753 [TBL] [Abstract][Full Text] [Related]
15. Prediction of the Effects of Missense Mutations on Human Myeloperoxidase Protein Stability Using In Silico Saturation Mutagenesis. Sobitan A; Edwards W; Jalal MS; Kolawole A; Ullah H; Duttaroy A; Li J; Teng S Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011324 [TBL] [Abstract][Full Text] [Related]
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17. Myeloperoxidase deficiency. Increased sensitivity for immunocytochemical compared to cytochemical detection of enzyme. Ross DW; Kaplow LS Arch Pathol Lab Med; 1985 Nov; 109(11):1005-6. PubMed ID: 2996459 [TBL] [Abstract][Full Text] [Related]